Skip to main content
. Author manuscript; available in PMC: 2016 Jul 1.
Published in final edited form as: Arthritis Rheumatol. 2015 Jul;67(7):1837–1847. doi: 10.1002/art.39111

Table 3.

Multivariate regression analysis of predictors of outcome on Likert scale (excluding resolution) (column A) and resolution (column B) of any mood disorder regardless of attribution.

Predictors A: Analysis of Likert scale outcome (excluding resolution) B: Analysis of time to resolution
Est. 95% CI P HR 95% CI P
Gender Female 0.20 −0.26 0.66 0.3985
Age at SLE diagnosis 0.805 0.637 1.019 0.0711
Location US −0.39 −1.64 0.85 0.0003 0.565 0.211 1.518 0.0125
Mexico 0.52 −0.82 1.85 0.793 0.288 2.187
Europe 0.73 −0.55 2.01 0.551 0.203 1.496
Canada 0.33 −0.95 1.62 1.160 0.438 3.078
Asia 0 1
Anti-depressant 0.51 0.12 0.90 0.0096
Immunosuppressive 0.55 0.20 0.91 0.0031
Any ongoing NP events in central/peripheral clusters by attribution* Central, SLE attributed −0.39 −0.83 0.04 0.0294 0.693 0.424 1.133 0.0183
Central, non-SLE attributed −0.52 −0.93 −0.12 0.595 0.394 0.898
Peripheral, SLE attributed 0.26 −0.94 1.46 1.540 0.728 3.258
Peripheral, non-SLE attributed −1.01 −2.02 −0.01 Not estimable
No NP events 0 1
Time since mood disorder onset 5+ years −0.30 −0.74 0.14 0.3168
4–5 years 0.05 −0.40 0.50
2–3 years 0.10 −0.26 0.45
<=1 year 0 0 0
*

Central, SLE attributed: patients with one or more ongoing central SLE attributed events at current visit

Central, non-SLE attributed: patients with one or more ongoing central non-SLE attributed events, but no ongoing central SLE-attributed events

Peripheral, SLE attributed: Patients with ongoing peripheral events only, of which one or more were SLE-attributed

Peripheral, non-SLE attributed: Patients with ongoing peripheral non-SLE attributed events only

No NP: patients without any ongoing NP events at current visit